Publications
Found 301 results
Author Title [ Type] Year Filters: First Letter Of Last Name is K [Clear All Filters]
A General Regioselective Approach to 2,4-Disubstituted Pyrimidin-5-yl C-2-Deoxyribonucleosides. Synthesis 2012, 44 (06), 953-965 DOI: 10.1055/s-0031-1289694.
Galactosyl Pentadecene Reversibly Enhances Transdermal and Topical Drug Delivery. Pharmaceutical Research 2017, 34 (10), 2097-2108 DOI: 10.1007/s11095-017-2214-3.
Galactosyl Pentadecene Reversibly Enhances Transdermal and Topical Drug Delivery. Pharmaceutical Research 2017, 34 (10), 2097-2108 DOI: 10.1007/s11095-017-2214-3.
Formal Total Synthesis of (±)-Estrone and Zirconocene-Promoted Cyclization of 2-Fluoro-1,7-octadienes and Ru-Catalyzed Ring Closing Metathesis. The Journal of Organic Chemistry 2008, 73 (16), 6202-6206 DOI: 10.1021/jo800620d.
Fluorescent Sulphur- and Nitrogen-Containing Porous Polymers with Tuneable Donor-Acceptor Domains for Light-Driven Hydrogen Evolution. Chemistry-a European Journal 2018, 24 (46), 11916-11921 DOI: 10.1002/chem.201802902.
Flexible double-headed cytosine-linked 2′-deoxycytidine nucleotides. Synthesis, polymerase incorporation to DNA and interaction with DNA methyltransferases. Bioorganic & Medicinal Chemistry 2016, 24 (6), 1268-1276 DOI: 10.1016/j.bmc.2016.01.057.
Flavin–cyclodextrin conjugates: effect of the structure on the catalytic activity in enantioselective sulfoxidations. Tetrahedron: Asymmetry 2012, 23 (22–23), 1571-1583 DOI: 10.1016/j.tetasy.2012.10.017.
Fe-Catalyzed reactions of 2-chloro-1,7-dienes and allylmalonates. Tetrahedron Letters 2007, 48 (26), 4539-4541 DOI: 10.1016/j.tetlet.2007.04.143.
Extension of the Library of Biologically Active γ-Alkylidene Butenolides. Synthesis 2008, 2008 (21), 3465-3472 DOI: 10.1055/s-0028-1083181.
Exploring the "Goldilocks Zone" of Semiconducting Polymer Photocatalysts by Donor-Acceptor Interactions. Angewandte Chemie-International Edition 2018, 57 (43), 14188-14192 DOI: 10.1002/anie.201809702.
Exploring the "Goldilocks Zone" of Semiconducting Polymer Photocatalysts by Donor-Acceptor Interactions. Angewandte Chemie-International Edition 2018, 57 (43), 14188-14192 DOI: 10.1002/anie.201809702.
Exploring Supramolecular Gels in Flow-Type Chemistry-Design and Preparation of Stationary Phases. Industrial and Engineering Chemistry Research 2021, 60 (28), 10056-10063.
Examination of small molecule losses in 5-methylpyranopelargonidin MS/MS CID spectra by DFT calculations: MS/MS and DFT of 5-methylpyranopelargonidin. Journal of Mass Spectrometry 2014, 49 (12), 1314-1321 DOI: 10.1002/jms.3466.
Enantioselective Synthesis of the Unsaturated Fragment of Callyspongiolide. Organic Letters 2016, 18 (21), 5656-5659 DOI: 10.1021/acs.orglett.6b02897.
Enantioselective Synthesis of the Unsaturated Fragment of Callyspongiolide. Organic Letters 2016, 18 (21), 5656-5659 DOI: 10.1021/acs.orglett.6b02897.
Enantioselective Synthesis of (-)-Methoxyestrone. European Journal of Organic Chemistry 2011, 2011 (18), 3279-3282 DOI: 10.1002/ejoc.201100317.
Enantioselective PCCP Brønsted acid-catalyzed aminalization of aldehydes. Beilstein Journal of Organic Chemistry 2021, 17 (September), 2433-2440.
Enantioselective Organocatalytic Synthesis of 1,2,3-Trisubstituted Cyclopentanes. European Journal of Organic Chemistry 2021, 2021 (36), 5080-5089.
Enantioselective epoxide ring opening catalyzed by bis(tetrahydroisoquinoline) N,N′-dioxides. Collection of Czechoslovak Chemical Communications 2011, 76 (5), 415-422 DOI: 10.1135/cccc2011024.
Enantioselective epoxide ring opening catalyzed by bis(tetrahydroisoquinoline) N,N′-dioxides. Collection of Czechoslovak Chemical Communications 2011, 76 (5), 415-422 DOI: 10.1135/cccc2011024.
Enantioselective Allylation of β-Haloacrylaldehydes: Formal Total Syntheses of Pteroenone and Antillatoxin. European Journal of Organic Chemistry 2016, 2016 (12), 2110-2114 DOI: 10.1002/ejoc.201600286.
Enantioselective Allylation of β-Haloacrylaldehydes: Formal Total Syntheses of Pteroenone and Antillatoxin. European Journal of Organic Chemistry 2016, 2016 (12), 2110-2114 DOI: 10.1002/ejoc.201600286.
Enantioselective Allylation of Thiophene-2-carbaldehyde: Formal Total Synthesis of Duloxetine. Advanced Synthesis & Catalysis 2014, 356 (1), 199-204 DOI: 10.1002/adsc.201300849.
Enantioselective Allylation of tert-Butyldimethylsilyl-Protected Vanillin and Synthesis of a Lignan Derivative Isolated from Machilus wangchiana. European Journal of Organic Chemistry 2014, 2014 (34), 7556-7560 DOI: 10.1002/ejoc.201403094.
Enantioselective Allylation of tert-Butyldimethylsilyl-Protected Vanillin and Synthesis of a Lignan Derivative Isolated from Machilus wangchiana. European Journal of Organic Chemistry 2014, 2014 (34), 7556-7560 DOI: 10.1002/ejoc.201403094.